• AAMI ISO 10993-5 : 2009

    Superseded A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

    BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 5: TESTS FOR IN VITRO CYTOTOXICITY

    Available format(s):  Hardcopy, PDF

    Superseded date:  31-08-2021

    Language(s):  English

    Published date:  01-01-2014

    Publisher:  Association for the Advancement of Medical Instrumentation

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    Table of Contents - (Show below) - (Hide below)

    Glossary of equivalent standards
    Committee representation
    Background of AAMI adoption of ISO 10993-5:2009
    Foreword
    Introduction
    1 Scope
    2 Normative references
    3 Terms and definitions
    4 Sample and control preparation
       4.1 General
       4.2 Preparation of liquid extracts of material
       4.3 Preparation of material for direct-contact tests
       4.4 Preparation of controls
    5 Cell lines
    6 Culture medium
    7 Preparation of cell stock culture
    8 Test procedures
       8.1 Number of replicates
       8.2 Test on extracts
       8.3 Test by direct contact
       8.4 Test by indirect contact
       8.5 Determination of cytotoxicity
    9 Test report
    10 Assessment of results
    Annex A (informative) Neutral red uptake (NRU) cytotoxicity
            test
    Annex B (informative) Colony formation cytotoxicity test
    Annex C (informative) MTT cytotoxicity test
    Annex D (informative) XTT cytotoxicity test
    Bibliography

    Abstract - (Show below) - (Hide below)

    Specifies test methods to assess the in vitro cytotoxicity of medical devices.

    General Product Information - (Show below) - (Hide below)

    Committee WG 05
    Document Type Standard
    Product Note Reconfirmed 2009
    Publisher Association for the Advancement of Medical Instrumentation
    Status Superseded
    Superseded By

    Standards Referencing This Book - (Show below) - (Hide below)

    ISO 10993-12:2012 Biological evaluation of medical devices Part 12: Sample preparation and reference materials
    ISO 10993-1:2009 Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
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